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      The Prevotella copri Complex Comprises Four Distinct Clades Underrepresented in Westernized Populations

      research-article
      1 , , 1 , 2 , 1 , 3 , 1 , 19 , 1 , 1 , 1 , 4 , 6 , 1 , 6 , 7 , 8 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 15 , 16 , 3 , 17 , 18 , 6 , 7 , 2 , 4 , 5 , 15 , 1 , 20 , ∗∗
      Cell Host & Microbe
      Cell Press
      human microbiome, metagenomics, Prevotella copri, comparative microbial genomics, ancient DNA, gut microbes, metagenomic assembly, Westernization, bacterial pangenome, bacterial phylogenetics, Iceman

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          Summary

          Prevotella copri is a common human gut microbe that has been both positively and negatively associated with host health. In a cross-continent meta-analysis exploiting >6,500 metagenomes, we obtained >1,000 genomes and explored the genetic and population structure of P. copri. P. copri encompasses four distinct clades (>10% inter-clade genetic divergence) that we propose constitute the  P. copri complex, and all clades were confirmed by isolate sequencing. These clades are nearly ubiquitous and co-present in non-Westernized populations. Genomic analysis showed substantial functional diversity in the complex with notable differences in carbohydrate metabolism, suggesting that multi-generational dietary modifications may be driving reduced prevalence in Westernized populations. Analysis of ancient metagenomes highlighted patterns of P. copri presence consistent with modern non-Westernized populations and a clade delineation time pre-dating human migratory waves out of Africa. These findings reveal that P. copri exhibits a high diversity that is underrepresented in Western-lifestyle populations.

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          Highlights

          • P. copri is not a monotypic species but composed of four distinct clades

          • The P. copri complex is more prevalent in populations with non-Westernized lifestyles

          • P. copri clades are frequently co-present within non-Westernized individuals

          • Ancient stool samples suggest Westernization leads to P. copri underrepresentation

          Abstract

          Tett et al. find that the intestinal microbe Prevotella copri encompasses four distinct clades constituting the P. copri complex. The complex is prevalent in non-Westernized populations where co-presence of all clades is commonly observed within individuals. Analysis of ancient stool samples supports Westernization as contributing to reduced P. copri prevalence.

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          Most cited references60

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          Dietary Fiber-Induced Improvement in Glucose Metabolism Is Associated with Increased Abundance of Prevotella.

          The gut microbiota plays an important role in human health by interacting with host diet, but there is substantial inter-individual variation in the response to diet. Here we compared the gut microbiota composition of healthy subjects who exhibited improved glucose metabolism following 3-day consumption of barley kernel-based bread (BKB) with those who responded least to this dietary intervention. The Prevotella/Bacteroides ratio was higher in responders than non-responders after BKB. Metagenomic analysis showed that the gut microbiota of responders was enriched in Prevotella copri and had increased potential to ferment complex polysaccharides after BKB. Finally, germ-free mice transplanted with microbiota from responder human donors exhibited improved glucose metabolism and increased abundance of Prevotella and liver glycogen content compared with germ-free mice that received non-responder microbiota. Our findings indicate that Prevotella plays a role in the BKB-induced improvement in glucose metabolism observed in certain individuals, potentially by promoting increased glycogen storage.
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            Ancient human genomes suggest three ancestral populations for present-day Europeans

            We sequenced genomes from a $\sim$7,000 year old early farmer from Stuttgart in Germany, an $\sim$8,000 year old hunter-gatherer from Luxembourg, and seven $\sim$8,000 year old hunter-gatherers from southern Sweden. We analyzed these data together with other ancient genomes and 2,345 contemporary humans to show that the great majority of present-day Europeans derive from at least three highly differentiated populations: West European Hunter-Gatherers (WHG), who contributed ancestry to all Europeans but not to Near Easterners; Ancient North Eurasians (ANE), who were most closely related to Upper Paleolithic Siberians and contributed to both Europeans and Near Easterners; and Early European Farmers (EEF), who were mainly of Near Eastern origin but also harbored WHG-related ancestry. We model these populations' deep relationships and show that EEF had $\sim$44% ancestry from a "Basal Eurasian" lineage that split prior to the diversification of all other non-African lineages.
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              Massive migration from the steppe was a source for Indo-European languages in Europe

              We generated genome-wide data from 69 Europeans who lived between 8,000-3,000 years ago by enriching ancient DNA libraries for a target set of almost 400,000 polymorphisms. Enrichment of these positions decreases the sequencing required for genome-wide ancient DNA analysis by a median of around 250-fold, allowing us to study an order of magnitude more individuals than previous studies and to obtain new insights about the past. We show that the populations of Western and Far Eastern Europe followed opposite trajectories between 8,000-5,000 years ago. At the beginning of the Neolithic period in Europe, ∼8,000-7,000 years ago, closely related groups of early farmers appeared in Germany, Hungary and Spain, different from indigenous hunter-gatherers, whereas Russia was inhabited by a distinctive population of hunter-gatherers with high affinity to a ∼24,000-year-old Siberian. By ∼6,000-5,000 years ago, farmers throughout much of Europe had more hunter-gatherer ancestry than their predecessors, but in Russia, the Yamnaya steppe herders of this time were descended not only from the preceding eastern European hunter-gatherers, but also from a population of Near Eastern ancestry. Western and Eastern Europe came into contact ∼4,500 years ago, as the Late Neolithic Corded Ware people from Germany traced ∼75% of their ancestry to the Yamnaya, documenting a massive migration into the heartland of Europe from its eastern periphery. This steppe ancestry persisted in all sampled central Europeans until at least ∼3,000 years ago, and is ubiquitous in present-day Europeans. These results provide support for a steppe origin of at least some of the Indo-European languages of Europe.
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                Author and article information

                Contributors
                Journal
                Cell Host Microbe
                Cell Host Microbe
                Cell Host & Microbe
                Cell Press
                1931-3128
                1934-6069
                13 November 2019
                13 November 2019
                : 26
                : 5
                : 666-679.e7
                Affiliations
                [1 ]CIBIO Department, University of Trento, 38123 Trento, Italy
                [2 ]Department of Sustainable Agro-Ecosystems and Bioresources, Fondazione Edmund Mach, 1 38010 S, San Michele all'Adige, Italy
                [3 ]Kimmel Center for Biology and Medicine of the Skirball Institute, New York University School of Medicine, New York, NY 10016, USA
                [4 ]The Broad Institute of MIT and Harvard, Cambridge, MA 02115, USA
                [5 ]Biostatistics Department, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA
                [6 ]Department of Agricultural Sciences, University of Naples “Federico II”, Portici, Italy
                [7 ]Task Force on Microbiome Studies, University of Naples “Federico II”, Naples, Italy
                [8 ]Center for Computational Biology, Flatiron Institute, New York, NY 10010, USA
                [9 ]Departments of Biology and Computer Science, New York University, New York, NY 10003, USA
                [10 ]National Institute for Medical Research, Tanga Centre, Tanzania
                [11 ]Kumasi Centre for Collaborative Research in Tropical Medicine, Kwame Nkrumah University of Science and Technology, Ghana
                [12 ]Hardin Hall, School of Natural Resources, University of Nebraska, Lincoln, NE 68583-0987, USA
                [13 ]CUBE - Division of Computational Systems Biology, Department of Microbiology and Ecosystem Science, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria
                [14 ]Centre for Translational Microbiome Research, Department of Microbiology Tumor and Cell Biology, Karolinska Institutet, 171 65 Solna, Stockholm, Sweden
                [15 ]Institute for Mummy Studies, EURAC Research, Viale Druso 1, 39100 Bolzano, Italy
                [16 ]Institute of Agrochemistry and Food Technology, National Research Council (IATA-CSIC), 46980 Paterna, Valencia, Spain
                [17 ]Department of Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany
                [18 ]German Center for Infection Research, Hamburg-Borstel-Lübeck-Riems, 20359 Hamburg, Germany
                Author notes
                []Corresponding author adrianjames.tett@ 123456unitn.it
                [∗∗ ]Corresponding author nicola.segata@ 123456unitn.it
                [19]

                Present address: Department of Agricultural Sciences, University of Naples “Federico II,” Portici, Italy

                [20]

                Lead Contact

                Article
                S1931-3128(19)30427-5
                10.1016/j.chom.2019.08.018
                6854460
                31607556
                1faf7484-2251-4399-b270-66bc117e7495
                © 2019 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 April 2019
                : 5 July 2019
                : 28 August 2019
                Categories
                Article

                Microbiology & Virology
                human microbiome,metagenomics,prevotella copri,comparative microbial genomics,ancient dna,gut microbes,metagenomic assembly,westernization,bacterial pangenome,bacterial phylogenetics,iceman

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